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trFluor™ Eu Acceptor XL665-Streptavidin Conjugate

Product key features

  • Readily used for developing TR-FRET assays
  • Conveniently used to bind to a biotinylated probe
  • Perfectly paired with an Eu-dye-labeled analyte (e.g., an antibody, or antigen)
  • TR-FRET assays have low back ground and high sensitivity

Product description

trFluor™ Eu Acceptor XL665-Streptavidin Conjugate is an excellent building block for developing TR-FRET assays. It is labeled with the trFluor™ Eu Acceptor XL665 that is an excellent replacement for the D2 acceptor. The acceptor is commonly used to label antibodies or antigens to prepare the bioconjugates that are used to pair with Eu-labeled probes for developing TR-FRET assays. trFluor™ Eu Acceptor XL665-Streptavidin Conjugate can be readily used with a biotinylated Eu luminescent probe such as antibodies. Eu probes enable time-resolved fluorometry (TRF) for the assays that require high sensitivity. They have large Stokes shifts and extremely long emission half-lives when compared to more traditional fluorophores such as Alexa Fluor or cyanine dyes. Compared to the other TRF compounds, our TR Fluor™ Eu probes have relatively high stability, high emission yield and ability to be linked to biomolecules. The trFluor™ Eu probes are excellent donors for developing TR-FRET assays by pairing with trFluor™ Eu Acceptor XL665-Streptavidin Conjugate. Many biological compounds present in cells, serum or other biological fluids are naturally fluorescent, and thus the use of conventional, prompt fluorophores lead to serious limitations in assay sensitivity due to the high background caused by the autofluorescence of the biological molecules to be assayed. The use of long-lived fluorophores combined with time-resolved detection (a delay between excitation and emission detection) minimizes prompt fluorescence interferences.

Spectrum

References

View all 50 references: Citation Explorer
Protocol for the comprehensive biochemical and cellular profiling of small-molecule degraders using CoraFluor TR-FRET technology.
Authors: Payne, N Connor and Ichikawa, Saki and Woo, Christina M and Mazitschek, Ralph
Journal: STAR protocols (2024): 103129
Development of a high-throughput TR-FRET screening assay for a fast-cycling KRAS mutant.
Authors: Larson, Jacob E and Hardy, P Brian and Schomburg, Noah K and Wang, Xiaodong and Kireev, Dmitri and Rossman, Kent L and Pearce, Kenneth H
Journal: SLAS discovery : advancing life sciences R & D (2023): 39-47
Homogeneous Time-Resolved Fluorescence Resonance Energy Transfer (TR-FRET) Cofactor Recruitment Assay for PPARα and PPARγ.
Authors: Roth, Doris and Benz, Jörg and Grether, Uwe and Dietz, Michel
Journal: Methods in molecular biology (Clifton, N.J.) (2023): 155-169
Deep Drug Discovery of Mac Domain of SARS-CoV-2 (WT) Spike Inhibitors: Using Experimental ACE2 Inhibition TR-FRET Assay, Screening, Molecular Dynamic Simulations and Free Energy Calculations.
Authors: Iqbal, Saleem and Lin, Sheng-Xiang
Journal: Bioengineering (Basel, Switzerland) (2023)
Development of a high-throughput TR-FRET screening assay for LAG-3/FGL1 interaction.
Authors: Abdel-Rahman, Somaya A and Zhang, Longfei and Gabr, Moustafa T
Journal: SLAS discovery : advancing life sciences R & D (2023): 188-192
Page updated on March 11, 2025

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Catalog Number1441
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Physical properties

Solvent

Water

Spectral properties

Excitation (nm)

652

Emission (nm)

659

Storage, safety and handling

H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22

Storage

Freeze (< -15 °C); Minimize light exposure